HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 67467008, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 67462280 | HCID 67462280 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67467008 | HCID 67467008 | 89% |
Reaction Steps
To a solution of (5-bromo-4-ethylthiazol-2-yl)methanol (313 mg 1.41 mmol) in THF (15 ml) under nitrogen at room temperature was added thionyl chloride (0.206 ml 2.82 mmol) and stirred overnight. LCMS indicated the completion of the reaction. A saturated ice cold aqueous NaHCO3 solution was added to the reaction solution with gas evolution. The mixture was extracted with EtOAc (4×20 ml), dried over sodium sulfate and concentrated to give a brown oil 301 mg, 89% which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916593B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-c9d3e2c4307042a7b2604437d074a682 |
| Source note | uspto-grants-2014_12 |